Variant report

Variant	nsv432744
Chromosome Location	chr5:37374124-37743077
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3652)
CpG islands
(count:1224)
Chromatin interactive
region (count:144)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3652 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:37566412-37566482	K562	blood:	n/a	n/a
2	ARID3A	chr5:37379206-37379473	K562	blood:	n/a	n/a
3	ARID3A	chr5:37413045-37413386	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:37555087-37555396	K562	blood:	n/a	n/a
5	ARID3A	chr5:37435813-37436000	K562	blood:	n/a	chr5:37435891-37435907
6	ARID3A	chr5:37412949-37413405	K562	blood:	n/a	n/a
7	ARID3A	chr5:37424736-37424788	HepG2	liver:	n/a	n/a
8	ARID3A	chr5:37723622-37723741	HepG2	liver:	n/a	n/a
9	ARID3A	chr5:37552742-37553918	K562	blood:	n/a	n/a
10	ARID3A	chr5:37723042-37723269	HepG2	liver:	n/a	n/a
11	ARID3A	chr5:37554224-37554305	K562	blood:	n/a	n/a
12	ARID3A	chr5:37717456-37718839	HepG2	liver:	n/a	chr5:37718035-37718051
13	ARID3A	chr5:37668578-37669026	HepG2	liver:	n/a	n/a
14	ARID3A	chr5:37561556-37561928	K562	blood:	n/a	n/a
15	ARID3A	chr5:37435399-37435833	HepG2	liver:	n/a	n/a
16	ARID3A	chr5:37576244-37577007	K562	blood:	n/a	chr5:37576689-37576705 chr5:37576688-37576704
17	ARID3A	chr5:37725466-37725597	HepG2	liver:	n/a	n/a
18	ARID3A	chr5:37723608-37723756	K562	blood:	n/a	n/a
19	ATF1	chr5:37614336-37614416	K562	blood:	n/a	n/a
20	ATF1	chr5:37723031-37723344	K562	blood:	n/a	n/a
21	ATF1	chr5:37379197-37379483	K562	blood:	n/a	n/a
22	ATF1	chr5:37668620-37669142	K562	blood:	n/a	n/a
23	ATF1	chr5:37576224-37576625	K562	blood:	n/a	n/a
24	ATF1	chr5:37413139-37413402	K562	blood:	n/a	n/a
25	ATF1	chr5:37672268-37672700	K562	blood:	n/a	n/a
26	ATF1	chr5:37552974-37553744	K562	blood:	n/a	n/a
27	ATF2	chr5:37672199-37672626	GM12878	blood:	n/a	n/a
28	ATF2	chr5:37379058-37379502	GM12878	blood:	n/a	n/a
29	ATF2	chr5:37722807-37723371	GM12878	blood:	n/a	n/a
30	ATF2	chr5:37738072-37738628	GM12878	blood:	n/a	n/a
31	ATF2	chr5:37721531-37722125	GM12878	blood:	n/a	n/a
32	ATF2	chr5:37379198-37379480	H1-hESC	embryonic stem cell:	n/a	n/a
33	ATF2	chr5:37738148-37738641	GM12878	blood:	n/a	n/a
34	ATF2	chr5:37722812-37723380	GM12878	blood:	n/a	n/a
35	ATF3	chr5:37668695-37668903	K562	blood:	n/a	n/a
36	ATF3	chr5:37379172-37379508	A549	lung:	n/a	n/a
37	ATF3	chr5:37668466-37669039	A549	lung:	n/a	n/a
38	ATF3	chr5:37413096-37413476	K562	blood:	n/a	n/a
39	ATF3	chr5:37668562-37669111	HCT-116	colon:	n/a	n/a
40	ATF3	chr5:37379100-37379507	A549	lung:	n/a	n/a
41	ATF3	chr5:37722947-37723383	K562	blood:	n/a	n/a
42	ATF3	chr5:37668528-37669122	HCT-116	colon:	n/a	n/a
43	ATF3	chr5:37668523-37668997	K562	blood:	n/a	n/a
44	ATF3	chr5:37379108-37379491	K562	blood:	n/a	n/a
45	BACH1	chr5:37512136-37512171	K562	blood:	n/a	n/a
46	BACH1	chr5:37637658-37637891	H1-hESC	embryonic stem cell:	n/a	chr5:37637759-37637773
47	BACH1	chr5:37553100-37553687	K562	blood:	n/a	n/a
48	BATF	chr5:37721677-37722017	GM12878	blood:	n/a	chr5:37721867-37721878
49	BATF	chr5:37738147-37738489	GM12878	blood:	n/a	n/a
50	BATF	chr5:37721687-37721984	GM12878	blood:	n/a	chr5:37721867-37721878

(count:1224 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:37379358-37379408	HCF	heart:	n/a
2	chr5:37723683-37723733	AoSMC	blood vessel:	n/a
3	chr5:37378229-37378279	AG09309	skin:	n/a
4	chr5:37721782-37721832	AoSMC	blood vessel:	n/a
5	chr5:37379358-37379408	HCF	heart:	n/a
6	chr5:37723683-37723733	AoSMC	blood vessel:	n/a
7	chr5:37378229-37378279	AG09309	skin:	n/a
8	chr5:37721782-37721832	AoSMC	blood vessel:	n/a
9	chr5:37379396-37379446	T-47D	breast:	n/a
10	chr5:37379822-37379872	GM06990	blood:	n/a
11	chr5:37379358-37379408	PFSK-1	brain:	n/a
12	chr5:37379272-37379322	AG10803	skin:	n/a
13	chr5:37638144-37638194	HCT-116	colon:	n/a
14	chr5:37666865-37666915	HAEpiC	amniotic membrane:	n/a
15	chr5:37379358-37379408	ECC-1	luminal epithelium:	n/a
16	chr5:37379269-37379319	Caco-2	colon:	n/a
17	chr5:37484025-37484075	HCF	heart:	n/a
18	chr5:37379822-37379872	HL-60	blood:	n/a
19	chr5:37379396-37379446	NHBE	bronchial:	n/a
20	chr5:37379358-37379408	HCPEpiC	choroid plexus:	n/a
21	chr5:37379396-37379446	MCF-7	breast:	n/a
22	chr5:37379358-37379408	BJ	skin:	n/a
23	chr5:37379822-37379872	HNPCEpiC	eye:	n/a
24	chr5:37382801-37382851	PrEC	prostate:	n/a
25	chr5:37666865-37666915	K562	blood:	n/a
26	chr5:37379272-37379322	HMEC	breast:	n/a
27	chr5:37378272-37378322	NB4	blood:	n/a
28	chr5:37378050-37378100	AG04450	lung:	fetal
29	chr5:37484025-37484075	HL-60	blood:	n/a
30	chr5:37378229-37378279	NHBE	bronchial:	n/a
31	chr5:37378360-37378410	AoSMC	blood vessel:	n/a
32	chr5:37666865-37666915	PrEC	prostate:	n/a
33	chr5:37379822-37379872	AG09309	skin:	n/a
34	chr5:37379267-37379317	HNPCEpiC	eye:	n/a
35	chr5:37379396-37379446	HepG2	liver:	n/a
36	chr5:37379358-37379408	GM06990	blood:	n/a
37	chr5:37379358-37379408	HUVEC	blood vessel:	n/a
38	chr5:37378272-37378322	HUVEC	blood vessel:	n/a
39	chr5:37638144-37638194	SKMC	muscle:	n/a
40	chr5:37379461-37379511	SK-N-MC	brain:	n/a
41	chr5:37723683-37723733	MCF10A-Er-Src	breast:	n/a
42	chr5:37723683-37723733	GM12891	blood:	n/a
43	chr5:37379461-37379511	IMR90	lung:	fetal
44	chr5:37717768-37717818	ovcar-3	ovarian:	n/a
45	chr5:37721782-37721832	LNCaP	prostate:	n/a
46	chr5:37378050-37378100	HRCEpiC	kidney:	n/a
47	chr5:37723683-37723733	HMEC	breast:	n/a
48	chr5:37379358-37379408	GM12891	blood:	n/a
49	chr5:37378229-37378279	HNPCEpiC	eye:	n/a
50	chr5:37723683-37723733	AG04450	lung:	fetal

(count:144 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr5:37717152..37719759-chr5:37721474..37723768,2	K562	blood:
2	chr5:37395673..37397370-chr5:37410862..37413241,2	MCF-7	breast:
3	chr5:37583782..37585545-chr5:37586859..37589248,2	K562	blood:
4	chr5:37488881..37490858-chr5:37567347..37569058,2	K562	blood:
5	chr5:37659630..37663695-chr5:37665450..37669812,5	K562	blood:
6	chr5:37569124..37569718-chr8:118852447..118853416,2	MCF-7	breast:
7	chr5:37658934..37661849-chr5:37667178..37669216,3	MCF-7	breast:
8	chr5:37423699..37426165-chr5:37428640..37431370,2	MCF-7	breast:
9	chr5:37412738..37413377-chr5:38194610..38195311,2	MCF-7	breast:
10	chr5:37609718..37612103-chr5:37614733..37616548,2	K562	blood:
11	chr5:37630392..37632021-chr5:37637856..37640438,2	MCF-7	breast:
12	chr5:37702513..37704538-chr5:37716164..37718117,2	MCF-7	breast:
13	chr10:132633168..132634098-chr5:37613234..37613734,2	NB4	blood:
14	chr5:37713779..37717092-chr5:37718712..37720863,3	K562	blood:
15	chr5:37569701..37572288-chr5:37579867..37582083,2	MCF-7	breast:
16	chr5:37551924..37555267-chr5:37556271..37558320,3	K562	blood:
17	chr5:37412783..37413436-chr5:37723453..37724202,2	K562	blood:
18	chr5:37370064..37373071-chr5:37393227..37395634,3	K562	blood:
19	chr5:37477675..37480288-chr5:37486843..37489829,2	K562	blood:
20	chr5:37667989..37670619-chr5:37702239..37705026,2	MCF-7	breast:
21	chr5:37412852..37413708-chr5:37554717..37555628,3	MCF-7	breast:
22	chr5:37572624..37574156-chr5:37580736..37583153,2	K562	blood:
23	chr5:37578232..37579991-chr5:37581584..37583169,2	MCF-7	breast:
24	chr5:37379216..37379885-chr6:58287233..58287739,2	Hela-S3	cervix:
25	chr5:37536707..37538331-chr5:37538401..37541156,2	K562	blood:
26	chr5:37661443..37663164-chr5:37664838..37666948,2	MCF-7	breast:
27	chr5:37398413..37401041-chr5:37401249..37404698,3	K562	blood:
28	chr5:36875375..36878248-chr5:37375352..37377665,2	K562	blood:
29	chr5:37553408..37554969-chr5:37565315..37567049,2	K562	blood:
30	chr5:37550616..37553710-chr5:37559318..37562633,4	K562	blood:
31	chr5:37551824..37554603-chr5:37555317..37558093,4	K562	blood:
32	chr5:37392088..37394720-chr5:37398631..37400477,2	K562	blood:
33	chr5:37389025..37391631-chr5:37392336..37394905,2	K562	blood:
34	chr5:37543508..37545182-chr5:37552537..37554107,2	K562	blood:
35	chr5:37503334..37505446-chr5:37509179..37510910,2	K562	blood:
36	chr1:117601635..117602147-chr5:37379314..37380058,2	Hela-S3	cervix:
37	chr5:37413185..37413702-chr5:37723532..37724165,2	MCF-7	breast:
38	chr5:37496762..37498368-chr5:37500019..37501730,2	MCF-7	breast:
39	chr17:61358570..61359089-chr5:37412803..37413392,2	MCF-7	breast:
40	chr5:37370138..37373249-chr5:37374935..37377740,7	K562	blood:
41	chr5:37662824..37665076-chr5:37668148..37670201,3	MCF-7	breast:
42	chr5:37658934..37661849-chr5:37667178..37669216,3	MCF-7	breast:
43	chr5:37578232..37579991-chr5:37581584..37583169,2	MCF-7	breast:
44	chr5:37659630..37663695-chr5:37665450..37669812,5	K562	blood:
45	chr5:37711811..37713434-chr5:37718883..37721366,2	MCF-7	breast:
46	chr5:37711775..37713303-chr5:37715445..37717839,2	K562	blood:
47	chr5:37509914..37511896-chr5:37518755..37521412,2	K562	blood:
48	chr5:37565296..37570234-chr5:37571928..37578079,8	K562	blood:
49	chr5:37423699..37426165-chr5:37428640..37431370,2	MCF-7	breast:
50	chr5:37412825..37413381-chr5:37926629..37927147,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WDR70-4	chr5:37377986-37378073	NONHSAT101062
2	lnc-WDR70-4	chr5:37377151-37377385	NONHSAT101062
3	lnc-NIPBL-7	chr5:37379591-37379656	NONHSAT101065
4	lnc-NIPBL-7	chr5:37379404-37379494	NONHSAT101065
5	lnc-NIPBL-7	chr5:37381704-37381911	NONHSAT101065
6	lnc-NUP155-5	chr5:37505790-37506959	NONHSAT101066

No data

Variant related genes	Relation type
RNU6-1190P	TF binding region
ENSG00000250455	TF binding region
WDR70	TF binding region
ENSG00000248216	TF binding region
RNU6-484P	TF binding region
NUP155	TF binding region
RNU6-1190P	CpG island
ENSG00000250455	CpG island
WDR70	CpG island
ENSG00000248216	CpG island
RNU6-484P	CpG island
NUP155	CpG island
ENSG00000082068	chromatin interactions
ENSG00000248587	chromatin interactions
ENSG00000222743	chromatin interactions
ENSG00000164190	chromatin interactions
ENSG00000215190	chromatin interactions
ENSG00000183666	chromatin interactions
ENSG00000236137	chromatin interactions
ENSG00000113569	chromatin interactions

Extended variants
information (count: 13538 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:13538 , 50 per page) page: 1 2 3 4 5 6 7 ... 271

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10941327	chr5:37374124-37374125	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs567558320	chr5:37374130-37374131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs534974451	chr5:37374135-37374136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs564755123	chr5:37374165-37374166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs533467314	chr5:37374189-37374190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs376194498	chr5:37374198-37374199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs148024196	chr5:37374233-37374234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs546940450	chr5:37374261-37374262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs578141348	chr5:37374276-37374277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs373878690	chr5:37374326-37374327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs557572857	chr5:37374423-37374424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs575872319	chr5:37374531-37374532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs542973665	chr5:37374537-37374538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs183372	chr5:37374567-37374568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs566775792	chr5:37374661-37374662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs573596117	chr5:37374840-37374841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs62354999	chr5:37374847-37374848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs113938542	chr5:37374878-37374879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs368977077	chr5:37374944-37374945	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs559052268	chr5:37374962-37374963	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs529327949	chr5:37374998-37374999	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs532848979	chr5:37375019-37375020	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs549103647	chr5:37375036-37375037	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs551029360	chr5:37375049-37375050	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs190161416	chr5:37375056-37375057	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs534818877	chr5:37375058-37375059	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs568704879	chr5:37375090-37375091	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs549019016	chr5:37375099-37375100	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs192973646	chr5:37375121-37375122	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs528521404	chr5:37375128-37375129	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs546949006	chr5:37375154-37375155	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs34125297	chr5:37375160-37375161	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs547196644	chr5:37375174-37375175	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs150107532	chr5:37375178-37375179	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs539150031	chr5:37375207-37375208	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs113239554	chr5:37375234-37375235	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs184852299	chr5:37375327-37375328	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs569476247	chr5:37375344-37375345	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs536843509	chr5:37375365-37375366	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs138477542	chr5:37375402-37375403	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs4288140	chr5:37375443-37375444	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs557676083	chr5:37375448-37375449	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs142690228	chr5:37375449-37375450	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs188732807	chr5:37375450-37375451	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs551421431	chr5:37375524-37375525	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs573283687	chr5:37375560-37375561	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs369092043	chr5:37375625-37375626	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs141018516	chr5:37375638-37375639	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs544710457	chr5:37375639-37375640	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs563006886	chr5:37375702-37375703	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
Myofibroblastic sarcoma	19369631	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Non-small cell lung cancer	20864512	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Non-small cell lung cancer	19010865	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Prostate cancer	18632612	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	19553991	CNVD
Lung cancer	19553991	CNVD
Melanoma	19553991	CNVD
Ovarian cancer	19553991	CNVD
Prostate cancer	19553991	CNVD
Non-small cell lung cancer	17156491	CNVD
Breast cancer	17133270	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Lung cancer	19153074	CNVD
Cornelia de Lange syndrome	21085971	CNVD
Autism	21701786	CNVD
Cervical cancer	16585170	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	23813976	CNVD
Schizophrenia	21346763	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Breast cancer	21990379	CNVD
Schizophrenia	19197363	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:5113 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:37372200-37375600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr5:37372200-37378800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr5:37372600-37379000	Weak transcription	HepG2	liver
4	chr5:37372800-37376000	Weak transcription	K562	blood
5	chr5:37375600-37376200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr5:37376000-37376400	Enhancers	K562	blood
7	chr5:37376200-37379000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr5:37376400-37379000	Weak transcription	K562	blood
9	chr5:37378200-37378400	Enhancers	Dnd41	blood
10	chr5:37378400-37378800	Flanking Active TSS	Dnd41	blood
11	chr5:37378600-37378800	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr5:37378600-37378800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
13	chr5:37378600-37380200	Active TSS	Stomach Smooth Muscle	stomach
14	chr5:37378800-37379000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr5:37378800-37379000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
16	chr5:37378800-37379200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr5:37378800-37379800	Active TSS	Primary neutrophils fromperipheralblood	blood
18	chr5:37378800-37379800	Active TSS	Primary hematopoietic stem cells	blood
19	chr5:37378800-37379800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr5:37378800-37379800	Active TSS	Duodenum Mucosa	Duodenum
21	chr5:37378800-37379800	Active TSS	Monocytes-CD14+_RO01746	blood
22	chr5:37378800-37380000	Active TSS	iPS-15b Cell Line	embryonic stem cell
23	chr5:37378800-37380000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr5:37378800-37380000	Active TSS	Colon Smooth Muscle	Colon
25	chr5:37378800-37380000	Active TSS	Fetal Adrenal Gland	Adrenal Gland
26	chr5:37378800-37380000	Active TSS	Thymus	Thymus
27	chr5:37378800-37380000	Active TSS	Dnd41	blood
28	chr5:37378800-37380000	Active TSS	Hela-S3	cervix
29	chr5:37378800-37380000	Active TSS	Osteobl	bone
30	chr5:37378800-37380200	Active TSS	Breast Myoepithelial Primary Cells	Breast
31	chr5:37378800-37380200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr5:37378800-37380200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr5:37378800-37380200	Active TSS	Fetal Intestine Large	intestine
34	chr5:37378800-37380200	Active TSS	Skeletal Muscle Male	skeletal muscle
35	chr5:37378800-37380200	Active TSS	GM12878-XiMat	blood
36	chr5:37378800-37380200	Active TSS	HSMM	muscle
37	chr5:37379000-37379200	Flanking Active TSS	Primary B cells from peripheral blood	blood
38	chr5:37379000-37379200	Flanking Active TSS	Fetal Stomach	stomach
39	chr5:37379000-37379200	Flanking Active TSS	Fetal Thymus	thymus
40	chr5:37379000-37379400	Flanking Active TSS	Primary B cells from cord blood	blood
41	chr5:37379000-37379400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
42	chr5:37379000-37379400	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
43	chr5:37379000-37379400	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
44	chr5:37379000-37379400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr5:37379000-37379400	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
46	chr5:37379000-37379600	Active TSS	Primary T helper cells fromperipheralblood	blood
47	chr5:37379000-37379800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
48	chr5:37379000-37379800	Active TSS	Primary monocytes fromperipheralblood	blood
49	chr5:37379000-37379800	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
50	chr5:37379000-37379800	Active TSS	Primary T killer memory cells from peripheral blood	blood

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